A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451930



Internal ID18274522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86866859..87291715hg38UCSC Ensembl
Innerchr10:88626616..89051472hg19UCSC Ensembl
Innerchr10:88616596..89041452hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38424857
hg19424857
hg18424857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428236
Supporting Variants
SamplesNA18498
Known GenesADIRF, AGAP11, BMPR1A, FAM25A, FAM35A, GLUD1, MMRN2, NUTM2A, NUTM2A-AS1, SNCG
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nssv451930
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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